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Glynase
Glynase - 0009-0341-01 - (glyburide)
Drug Information of Glynase
| Product NDC: | 0009-0341 |
| Proprietary Name: | Glynase |
| Non Proprietary Name: | glyburide |
| Active Ingredient(s): | 1.5 mg/1 & nbsp; glyburide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Glynase
| Product NDC: | 0009-0341 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020051 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19920304 |
Package Information of Glynase
| Package NDC: | 0009-0341-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0009-0341-01) |
NDC Information of Glynase
| NDC Code | 0009-0341-01 |
| Proprietary Name | Glynase |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0009-0341-01) |
| Product NDC | 0009-0341 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | glyburide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19920304 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | GLYBURIDE |
| Strength Number | 1.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient] |
